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T16268Namitecan；化合物 T16268ST-1968；ST-1968
Namitecan is an effective inhibitor of topoisomerase I. It has antitumor property.
价 格：￥电议型 号：T16268产 地：中国大陆
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T15688L-771688；化合物L-771688SNAP 6383；SNAP 6383
L-771688 (SNAP 6383) is a novel potent and selective α1A-adrenoceptor antagonist with a Ki value of 0.43±0.02 nM.L-771688 KE is used for the treatment of benign prostatic hyperplasia.
价 格：￥电议型 号：T15688产 地：中国大陆
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T13908SZ1676；化合物 T13908SZ1676
SZ1676 is a derivative of SZ1677, which is an agent of neuromuscular blocking.
价 格：￥电议型 号：T13908产 地：中国大陆
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T13898SPD-473 citrate；化合物 T13898SPD-473 citrate
SPD-473 citrate is an inhibitior of serotonin/dopamine/norepinephrine reuptake.
价 格：￥电议型 号：T13898产 地：中国大陆
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T13888SLF；化合物 T13888SLF
SLF is a synthetic ligand for FK506-binding protein (FKBP)( with an affinity of 3.1 μM for FKBP51 and an IC50 of 0.22 μM for FKBP12). SLF can be used in the synthesis of PROTAC.
价 格：￥电议型 号：T13888产 地：中国大陆
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T13028Sulfamerazine D4；化合物 T13028Sulfamerazine D4
Sulfamerazine D4, a deuterium-labeled version of Sulfamerazine, acts as a sulfonamide antibacterial. It inhibits the bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA) for the binding site on dihydropteroate synthase.
价 格：￥电议型 号：T13028产 地：中国大陆
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T13008ST3932；化合物 T13008ST3932
ST3932 is a ST1535 metabolite, is a adenosine A2A receptor antagonist(Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively).
价 格：￥电议型 号：T13008产 地：中国大陆
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T12997SR-318；化合物SR-318SR-318
SR-318 potently inhibits the TNF-α release in whole blood (IC50 = 283 nM). SR-318 is a potent and highly selective inhibitor of p38 MAPK. The IC50 values are 5 nM, 32 nM and 6.11 μM for p38α, p38β and p38α/β, respectively.
价 格：￥电议型 号：T12997产 地：中国大陆
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T12978NSC-70220；化合物 T12978SOS1-IN-1；SOS1-IN-1
SOS1-IN-1 is an inhibitor of SOS1.
价 格：￥电议型 号：T12978产 地：中国大陆
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T12948Sodium Channel inhibitor 1；化合物 T12948Sodium Channel inhibitor 1
Sodium Channel inhibitor1 is a novel and selective voltage-gated sodium channel for pain treatment. (IC50 Value of 0.16 uM and 0.41 uM for Na v1.7, V hold-90mV and Na v1.7, V hold-90mV)
价 格：￥电议型 号：T12948产 地：中国大陆
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T12878Semaglutide TFA (910463-68-2 free base)；化合物 T12878Semaglutide TFA；Semaglutide TFA
Semaglutide TFA is a agonist of glucagon-like peptide-1 (GLP-1) receptor,with a potential for type 2 diabetes treatment.
价 格：￥电议型 号：T12878产 地：中国大陆
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T12868Sch412348；化合物 T12868Sch412348
Sch412348 is a potent competitive the human adenosine A2A receptor antagonist with Ki of 0.6 nM and has >1000-fold selectivity over all other adenosine receptors.
价 格：￥电议型 号：T12868产 地：中国大陆
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T12818S119-8；化合物S119-8S119-8
RN-18 antagonizes Vif function and inhibits HIV-1 replication only in the presence of A3G. RN-18 increases cellular A3G levels in a Vif-dependent manner and increases A3G incorporation into virions without inhibiting general proteasome-mediated protein degradation. RN-18 enhances Vif degradation only in the presence of A3G, reduces viral infectivity by increasing A3G incorporation into virions and enhances cytidine deamination of the viral genome.
价 格：￥电议型 号：T12818产 地：中国大陆
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T125465SNA 60-367-18；化合物 SNA 60-367-18SNA 60-367-18
SNA 60-367-18 is a useful organic compound for research related to life sciences. The catalog number is T125465 and the CAS number is 193738-78-2.
价 格：￥电议型 号：T125465产 地：中国大陆
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T125235Scrophularoside A8；化合物 Scrophularoside A8Scrophularoside A8
Scrophularoside A8 is a useful organic compound for research related to life sciences. The catalog number is T125235 and the CAS number is 240820-44-4.
价 格：￥电议型 号：T125235产 地：中国大陆
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T12178Nateglinide D5；化合物 T12178Senaglinide D5|||A4166 D5；Senaglinide D5|||A4166 D5
Nateglinide D5 is a deuterium labeled Nateglinide.
价 格：￥电议型 号：T12178产 地：中国大陆
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T10288Alogliptin (13CD3)；化合物 T10288SYR-322 (13CD3)；SYR-322 (13CD3)
Alogliptin (SYR-322) 13CD3 is the deuterium-labeled Alogliptin. Alogliptin is a selective inhibitor of DPP-4.
价 格：￥电议型 号：T10288产 地：中国大陆
